BORAGO NICOTIANA- borago nicotiana liquid 
Uriel Pharmacy Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

----------

Borago Nicotiana

Directions: FOR ORAL USE.

Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

Active Ingredients: Borago e fol. 3X, Carduus ben. ex herba 3X, Hamamelis e fol. 3X, Nicotiana e fol. 6X, Sapphire 8X, Aesculus e sem. 10X, Scorodite 10X

Inactive Ingredients: Water, Salt

Use: Temporary relief of varicose veins.

KEEP OUT OF REACH OF CHILDREN.

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.

Questions? Call 866.642.2858 Made by Uriel, East Troy, WI 53120 www.urielpharmacy.com

BoragoNicotianaAmpules

BORAGO NICOTIANA 
borago nicotiana liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-2077
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BORAGE (UNII: PB618V0K2W) (BORAGE - UNII:PB618V0K2W) BORAGE3 [hp_X]  in 1 mL
CENTAUREA BENEDICTA (UNII: 6L5ZL09795) (CENTAUREA BENEDICTA - UNII:6L5ZL09795) CENTAUREA BENEDICTA3 [hp_X]  in 1 mL
HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV) (HAMAMELIS VIRGINIANA LEAF - UNII:T07U1161SV) HAMAMELIS VIRGINIANA LEAF3 [hp_X]  in 1 mL
TOBACCO LEAF (UNII: 6YR2608RSU) (TOBACCO LEAF - UNII:6YR2608RSU) TOBACCO LEAF6 [hp_X]  in 1 mL
ALUMINUM OXIDE (UNII: LMI26O6933) (ALUMINUM OXIDE - UNII:LMI26O6933) ALUMINUM OXIDE8 [hp_X]  in 1 mL
HORSE CHESTNUT (UNII: 3C18L6RJAZ) (HORSE CHESTNUT - UNII:3C18L6RJAZ) HORSE CHESTNUT10 [hp_X]  in 1 mL
FERROUS ARSENATE (UNII: 129CO35H12) (FERROUS ARSENATE - UNII:129CO35H12) FERROUS ARSENATE10 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-2077-110 in 1 BOX09/01/2009
11 mL in 1 AMPULE; Type 1: Convenience Kit of Co-Package
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic09/01/2009
Labeler - Uriel Pharmacy Inc. (043471163)
Establishment
NameAddressID/FEIBusiness Operations
Uriel Pharmacy Inc.043471163manufacture(48951-2077)

Revised: 5/2018
Document Id: 6c7d910a-e0f8-191a-e053-2991aa0ae605
Set id: 306f9eee-877b-46ee-9a36-894fa321b3d3
Version: 2
Effective Time: 20180518
 
Uriel Pharmacy Inc.